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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551578생성일: 2026년 10월 26일

4-Methylmorpholine → (4-Isopropyl-piperazin-1-yl)-(5-piperidin-1-ylmethyl-pyridin-2-yl)-methanone

https://huagongshe.com/reaction/551578

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물5-(Methoxycarbonyl)pyridine-2-carboxylic acidHCID 314992—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물1-Isopropylpiperazine dihydrochlorideHCID 12268378—
반응물6-(4-Isopropyl-piperazine-1-carbonyl)-nicotinic acid methyl esterHCID 44515774—
용매DichloromethaneHCID 6344—
생성물AmmoniaHCID 2222%
생성물(4-Isopropyl-piperazin-1-yl)-(5-piperidin-1-ylmethyl-pyridin-2-yl)-methanoneHCID 2512615474%

반응 단계

6-(4-Isopropyl-piperazine-1-carbonyl)-nicotinic acid methyl ester. To a solution of pyridine-2,5-dicarboxylic acid 5-methyl ester (1.00 g, 5.50 mmol) and 1-isopropyl-piperazine dihydrochloride (1.20 g, 6.10 mmol) in DCM (100 mL) was added 1-hydroxybenzotriazole hydrate (HOBt, 1.10 g, 8.30 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC, 1.60 g, 8.30 mmol), and N-methyl morpholine (2.9 mL, 27.0 mmol). After 18 h, the reaction mixture was quenched with 1 N aq. NaHCO3 (50 mL) and extracted with DCM (3×50 mL). The organic layers were combined, dried (Na2SO4), and concentrated. Chromatography of the residue (SiO2; 2-5% 2 M NH3 in MeOH/DCM) gave the title compound (1.20 g, 74%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947718B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-d3e3bf082b0746e98c813168336111a5
출처 메모uspto-grants-2011_05